Lasecka Lidia, Bin-Tarif Abdelghani, Bridgen Anne, Juleff Nicholas, Waters Ryan A, Baron Michael D
The Pirbright Institute, Ash Road, Pirbright, Woking, Surrey GU24 0NF, United Kingdom.
School of Biomedical Sciences, University of Ulster, Cromore Road, Coleraine BT52 1SA, Northern Ireland, United Kingdom.
PLoS One. 2015 Apr 23;10(4):e0124966. doi: 10.1371/journal.pone.0124966. eCollection 2015.
Nairobi sheep disease virus (NSDV; also called Ganjam virus in India) is a bunyavirus of the genus Nairovirus. It causes a haemorrhagic gastroenteritis in sheep and goats with mortality up to 90%. The virus is closely related to the human pathogen Crimean-Congo haemorrhagic fever virus (CCHFV). Little is currently known about the biology of NSDV. We have generated specific antibodies against the virus nucleocapsid protein (N) and polymerase (L) and used these to characterise NSDV in infected cells and to study its distribution during infection in a natural host. Due to its large size and the presence of a papain-like protease (the OTU-like domain) it has been suggested that the L protein of nairoviruses undergoes an autoproteolytic cleavage into polymerase and one or more accessory proteins. Specific antibodies which recognise either the N-terminus or the C-terminus of the NSDV L protein showed no evidence of L protein cleavage in NSDV-infected cells. Using the specific anti-N and anti-L antibodies, it was found that these viral proteins do not fully colocalise in infected cells; the N protein accumulated near the Golgi at early stages of infection while the L protein was distributed throughout the cytoplasm, further supporting the multifunctional nature of the L protein. These antibodies also allowed us to gain information about the organs and cell types targeted by the virus in vivo. We could detect NSDV in cryosections prepared from various tissues collected post-mortem from experimentally inoculated animals; the virus was found in the mucosal lining of the small and large intestine, in the lungs, and in mesenteric lymph nodes (MLN), where NSDV appeared to target monocytes and/or macrophages.
内罗毕羊病病毒(NSDV;在印度也被称为甘贾姆病毒)是内罗毕病毒属的一种布尼亚病毒。它会引发绵羊和山羊的出血性肠胃炎,死亡率高达90%。该病毒与人类病原体克里米亚-刚果出血热病毒(CCHFV)密切相关。目前对内罗毕羊病病毒的生物学特性了解甚少。我们已制备出针对该病毒核衣壳蛋白(N)和聚合酶(L)的特异性抗体,并利用这些抗体对感染细胞中的内罗毕羊病病毒进行表征,以及研究其在天然宿主感染过程中的分布情况。由于其体积较大且存在一种类木瓜蛋白酶(OTU样结构域),有人提出内罗毕病毒属的L蛋白会自动催化裂解为聚合酶和一种或多种辅助蛋白。识别内罗毕羊病病毒L蛋白N端或C端的特异性抗体未显示出在感染内罗毕羊病病毒的细胞中有L蛋白裂解的迹象。利用特异性抗N和抗L抗体发现,这些病毒蛋白在感染细胞中并未完全共定位;N蛋白在感染早期聚集在高尔基体附近,而L蛋白分布于整个细胞质中,这进一步支持了L蛋白的多功能性质。这些抗体还使我们能够获取有关该病毒在体内靶向的器官和细胞类型的信息。我们能够在从实验接种动物死后采集的各种组织制备的冰冻切片中检测到内罗毕羊病病毒;在小肠和大肠的黏膜层、肺以及肠系膜淋巴结(MLN)中发现了该病毒,在内罗毕羊病病毒似乎靶向单核细胞和/或巨噬细胞。